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Current good manufacturing practice calibration

Calibration, in current Good Manufacturing Practices (GMP) terminology, refers to instrument qualification or performance verification... [Pg.7]

Calibration, in current Good Manufacturing Practices (cGMP) terminology, refers to instrument qualification or performance verification of the HPLC. Note that neither any internal instrumental adjustment nor detector response curve for quantitation is intended here as in the common usage of the terminology. In most pharmaceutical laboratories. [Pg.291]

The use of Mechanical Calibration of Dissolution Apparatus 1 and 2 - Current Good Manufacturing Practice (cGMP) (Draft). [Pg.266]

U.S. Food and Drug Administration. 2007. Guidance for industry the use of mechanical calibration of dissolution apparatus 1 and 2—current good manufacturing practice (cGMP). [Pg.280]

Having defined sensors, a discussion of the current Good Manufacturing Practice (cGMP) definitions for calibration and validation follows with a presentation for a proposal for a new model for validation practices within the scope of the Food and Drug Administration 21st Century cGMP Initiative [4],... [Pg.247]

With these factors in mind, it is good operating practice to use the manufacturer s recommendation as a starting point and then determine empirically the current which gives the optimum combination of signal-to-noise ratio and calibration linearity. The major consideration is not to exceed the maximum rated current. [Pg.28]


See other pages where Current good manufacturing practice calibration is mentioned: [Pg.1040]    [Pg.313]    [Pg.314]    [Pg.1690]    [Pg.1118]    [Pg.1618]    [Pg.869]    [Pg.514]   
See also in sourсe #XX -- [ Pg.157 ]




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